Histrionicotoxin 283A

Histrionicotoxins are a group of related toxins found in the skin of poison frogs from the family Dendrobatidae, notably Oophaga histrionica (formerly Dendrobates histrionicus), which are native to Colombia.[1] It is likely that, as with other poison frog alkaloids, histrionicotoxins are not manufactured by the amphibians, but absorbed from insects in their diet and stored in glands in their skin.[2][3] They are notably less toxic than other alkaloids found in poison frogs, yet their distinct structure acts as a neurotoxin by non-competitive inhibition of nicotinic acetylcholine receptors.[4]

History

The first record of histrionicotoxins dates to 1823 by Captain Charles Stuart Cochrane.[5] Cochrane was exploring the tropical rainforests around Colombia and Panama. His reports mention tribes of Indians who used poison tipped arrows and blowgun darts for hunting and war. Upon further exploration, Cochrane found that these Indians extracted the poison from the skins of the poison dart frog, then known as Dendrobates histrionicus. An account from his diary reads:

"[...] called rana de veneno by the Spanish, about three inches long, yellow on the back, with very large black eyes... those who use poison catch the frogs in the woods and confine them in a hollow cane where they regularly feed them until they want the poison, when they take the unfortunate reptile and pass a pointed piece of wood down his throat and out of one of his legs. This torture makes the poor frog perspire very much, especially on the back, which becomes covered in a white froth; this is the most powerful poison that he yields, and in this they dip or roll the tips of their arrows, which will preserve their destructive power for a year. Afterwards, below this white substance, appears a yellow oil, which is carefully scraped off, and retains its deadly influence for four to six months, according to the goodness (as they say) of the frog. By this means, from one frog sufficient poison is obtained for about fifty arrows."

Chemical properties

Histrionicotoxins are a class rather than a specific poison and this broad spectrum poses synthetic challenges. Structures of histrionicotoxins were characterized in 1971.[6] Since then, several synthetic studies and total syntheses have been carried out. Table 1 describes some of the many variations in histrionicotoxin alkaloids from the parent molecule (283A).[7]

A table describing a few variants of the arrow poison, histrionicotoxin.
A table describing a few variants of the arrow poison, histrionicotoxin.

Synthesis

Since characterization, the development of synthetic pathways to histrionicotoxin has been of interest to research groups due to its unusual functionality. The Kishi group proposed the first total synthesis of the parent 283A in 1985 using 89, a previously synthesized lactam used for the synthesis of other variants.[8] Treatment with acetic anhydride yielded 133 in quantitative yield. The cyclic enol ether 134 was formed through oxidative cleavage promoting intramolecular addition followed by a basic deprotection and dehydration. Bromination followed by dehydrobromination in methanol was then found to give an epimeric mixture of unsaturated 135. Hydrolysis, reduction and acetylation yielded 136. Formation of a thiolactam followed by condensation with ethyl bromoacetate gave 137. Selective deprotection of the allylic alcohol followed by oxidation gave 138. A Wittig reaction then generated a chloroalkene, which, upon base-promoted elimination of HCl, gave a terminal alkyne, which was subsequently protected to form 139. The olefinic function of 139 was first reduced using cyanoborohydride before further reduction of 140 to an epimeric mixture of alcohols. A retro-Michael addition was then performed under basic conditions at low temperature, successfully epimerising this compound to give the desired epimer 141. A reaction with triphenylphosphine then generated the phosphonium salt 142, and a Wittig reaction could then be performed to attach the silyl-protected cis-ene-yne function, which was then deprotected to yield the target (±)-HTX 283A.

25 Step Synthesis of HTX presented by the Kishi group in 1985.
25 Step Synthesis of HTX presented by the Kishi group in 1985.

Mechanism of action

HTX acts as a noncompetitive antagonist of nicotinic acetylcholine receptors, which are implicated in neural signaling. As a non-competitive antagonist, HTX binds to a subunit of the nicotinic acetylcholine receptor.3 This actually increases the affinity for the agonist acetylcholine and stabilizes the desensitized receptor.[9] This blocks action potentials and slows neural function. Histrionicotoxin has been shown to bind competitively with many local anesthetics, such as tetracaine, as well as other aromatic amine non-competitive antagonists of the receptors, indicating the compounds likely share a binding site; this site of interaction is located outside the transmembrane domain of the nicotinic acetylcholine receptor, though the exact interaction remains uncharacterized.[10][11] While histrionicotoxin does share a binding location with other non-competitive antagonists of the nicotinic acetylcholine receptor, it has been proven to have relatively higher affinity for desensitized receptors than phencyclidine, indicating further yet uncharacterized subtlety in the nature of its binding.[10] Additionally, studies of the effects of histrionicotoxin on end-plate potential have shown that the compound hinders membrane potential propagation, but has emergent characteristics with membrane hyperpolarizations.[12] The binding of histrionicotoxin is rapidly reversible, and so it can be readily removed from affected regions with repeated washing, or, in vivo, with natural bodily diffusion.[12] High concentrations of HTX have been demonstrated to have antagonistic effects on batrachotoxin.[13]

Toxicity

Histrionicotoxin is relatively not as toxic as other alkaloids from poison dart frogs. Preliminary tests showed that mice could survive a 5 mg/kg dose of histrionicotoxin 283a and recover within 3 hours with no lasting effects.[6]

See also

References

  1. ↑ Daly JW (1982). "Alkaloids of Neotropical Poison Frogs (Dendrobatidae)". Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Vol. 41. pp. 205–340. doi:10.1007/978-3-7091-8656-5_6. ISBN 978-3-7091-8658-9. PMID 7049875.
  2. ↑ Daly JW (January 1995). "The chemistry of poisons in amphibian skin". Proceedings of the National Academy of Sciences of the United States of America. 92 (1): 9–13. Bibcode:1995PNAS...92....9D. doi:10.1073/pnas.92.1.9. PMC 42808. PMID 7816854.
  3. ↑ Jones TH, Adams RM, Spande TF, Garraffo HM, Kaneko T, Schultz TR (November 2012). "Histrionicotoxin alkaloids finally detected in an ant". Journal of Natural Products. 75 (11): 1930–6. doi:10.1021/np300485v. PMID 23088730.
  4. ↑ Oberthür W, Muhn P, Baumann H, Lottspeich F, Wittmann-Liebold B, Hucho F (August 1986). "The reaction site of a non-competitive antagonist in the delta-subunit of the nicotinic acetylcholine receptor". The EMBO Journal. 5 (8): 1815–9. doi:10.1002/j.1460-2075.1986.tb04431.x. PMC 1167045. PMID 3758027.
  5. ↑ Edwards N, Reed M. "Histrionicotoxin from South American Poison-Dart Frogs". The Chemical Laboratories. Retrieved 3 June 2017.
  6. 1 2 Daly JW, Karle I, Myers CW, Tokuyama T, Waters JA, Witkop B (August 1971). "Histrionicotoxins: roentgen-ray analysis of the novel allenic and acetylenie spiroalkaloids isolated from a Colombian frog, Dendrobates histrionicus". Proceedings of the National Academy of Sciences of the United States of America. 68 (8): 1870–5. Bibcode:1971PNAS...68.1870D. doi:10.1073/pnas.68.8.1870. PMC 389311. PMID 5288773.
  7. ↑ Sinclair A, Stockman RA (April 2007). "Thirty-five years of synthetic studies directed towards the histrionicotoxin family of alkaloids". Natural Product Reports. 24 (2): 298–326. doi:10.1039/b604203c. PMID 17389999.
  8. ↑ Carey SC, Aratani M, Kishi Y (1985). "A total synthesis of d,1-histrionicotoxin". Tetrahedron Letters. 26 (48): 5887–5890. doi:10.1016/S0040-4039(00)98253-4.
  9. ↑ Burgermeister W, Catterall WA, Witkop B (December 1977). "Histrionicotoxin enhances agonist-induced desensitization of acetylcholine receptor". Proceedings of the National Academy of Sciences of the United States of America. 74 (12): 5754–8. Bibcode:1977PNAS...74.5754B. doi:10.1073/pnas.74.12.5754. PMC 431872. PMID 272000.
  10. 1 2 Gallagher MJ, Chiara DC, Cohen JB (June 2001). "Interactions between 3-(trifluoromethyl)-3-(m-[125I]iodophenyl)diazirine and tetracaine, phencyclidine, or histrionicotoxin in the Torpedo species nicotinic acetylcholine receptor ion channel". Molecular Pharmacology. 59 (6): 1514–22. doi:10.1124/mol.59.6.1514. PMID 11353813. S2CID 6637773.
  11. ↑ Johnson DA, Nuss JM (August 1994). "The histrionicotoxin-sensitive ethidium binding site is located outside of the transmembrane domain of the nicotinic acetylcholine receptor: a fluorescence study". Biochemistry. 33 (31): 9070–7. doi:10.1021/bi00197a007. PMID 8049208.
  12. 1 2 Masukawa LM, Albuquerque EX (September 1978). "Voltage- and time-dependent action of histrionicotoxin on the endplate current of the frog muscle". The Journal of General Physiology. 72 (3): 351–67. doi:10.1085/jgp.72.3.351. PMC 2228541. PMID 308995.
  13. ↑ Bartels-Bernal E, Diaz E, Cadena R, Ramos J, Daly JW (September 1983). "Effect of histrionicotoxin on ion channels in synaptic and conducting membranes of electroplax of Electrophorus electricus". Cellular and Molecular Neurobiology. 3 (3): 203–12. doi:10.1007/bf00710947. PMID 6322994. S2CID 30388813.
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